Tag | Content |
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EnhancerAtlas ID | HS060-16703 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:4083130-4084950 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr19:4084376-4084394 | TCTTCCTCCCTCCCTCCC | - | 6.36 | HSF1 | MA0486.2 | chr19:4084568-4084581 | TTCTAGAAGCTTC | + | 6.28 | MYCN | MA0104.4 | chr19:4084542-4084554 | GGCCACGTGGCC | + | 7.22 | MYCN | MA0104.4 | chr19:4084542-4084554 | GGCCACGTGGCC | - | 7.22 | Myod1 | MA0499.1 | chr19:4084615-4084628 | TGCAGCTGTCCCC | + | 7.12 | ZNF263 | MA0528.1 | chr19:4084371-4084392 | CCCCTTCTTCCTCCCTCCCTC | - | 6.14 | ZNF263 | MA0528.1 | chr19:4084310-4084331 | GGAAGAGGAGCGGAGGGAGGG | + | 6.48 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_00903 | chr19:4083864-4084455 | Adrenal_Gland | SE_02962 | chr19:4083523-4085082 | Bladder | SE_12453 | chr19:4083727-4085036 | CD3 | SE_19502 | chr19:4083630-4085257 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20194 | chr19:4083237-4085170 | CD56 | SE_22707 | chr19:4083615-4085191 | CD8_primiary | SE_23073 | chr19:4083139-4085071 | Colon_Crypt_1 | SE_23728 | chr19:4083583-4084973 | Colon_Crypt_2 | SE_24683 | chr19:4082893-4083451 | Colon_Crypt_3 | SE_24683 | chr19:4083592-4085030 | Colon_Crypt_3 | SE_26575 | chr19:4082693-4085061 | Esophagus | SE_27700 | chr19:4083659-4085066 | Fetal_Intestine | SE_28696 | chr19:4083692-4085120 | Fetal_Intestine_Large | SE_31428 | chr19:4083442-4085057 | Gastric | SE_42412 | chr19:4083527-4084881 | Lung | SE_50061 | chr19:4082762-4085231 | Sigmoid_Colon | SE_53358 | chr19:4083688-4084969 | Spleen | SE_55380 | chr19:4083851-4084635 | Thymus | SE_58113 | chr19:4083508-4084948 | VACO_9m | SE_62529 | chr19:4051126-4090382 | Tonsil | SE_65287 | chr19:4083611-4084987 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I004082 | chr19 | 4082946 | 4085145 |
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Enhancer Sequence | TGCCTTTAGC CCTTAGGGCG GCTATAAATT CTAATTTCTG GGCCCGAGCG AGCGCCGTGG 60 GGAGGCTGCA GGCTCCCCAG CGATGGACAG GGGCTCTTAT CTTTTAGGAT CCCACAGAGC 120 ACTGCAGAAA AGCCCCAAAT ATTTGTGGGT CACGAAGGCA GTGTCCTGTC AGGGGAGACA 180 GCAGGATGGT GGGACCACAG GATCGTCCAT GTCTTCCCTG GGGGAGGTTC GAGTCACCTT 240 CAGAAGGTCA CCTAACTTGC AGGGACTCCG CTGCCGCAGA GGTTGTGTGG GGAGAGGCAA 300 ACCTGGTCAG CCTATTTTGT GGGGTGCAAA CAGAAGGGAT GTGGGCCTCC TCGGAAGTCT 360 GCAGAGAGGA TTCGCTCCTC CGTGGACGCT TCTCTCTTTT CTTGAGCCTG TGATGAGTTC 420 CTTTGCAAAT AGGGAAACTG AGGCTCTCAG AGGGGATTCT ATCTTCCCCA AGGTCACAGG 480 CCCAAGGACA GCAGAAATAT CGTCAGGCCT GTGGTCCTGA TGTTCAAACA GGAGGCCCTG 540 GCTGGCCGCA GCGACTCACG CCTATAATCC CAGCACACTG GGATCAGAAG GATTGCTTGG 600 GGCCAGGAGT TCCAGGAGTT TCAGGCCAGC CTGGGCAATA CGGTGAGACC CCATCTCTAC 660 GAGAAAGTTT CAAAAAATGA GCTGGGCATG GTGGCGCGCG CCTGCAGTCC CAGTTACTCA 720 GGAGGCTGAG GCAGGAGGAT CGCTGGAACC TGGGAGGCGG AGGCTGAAGT GAGCTATGAT 780 GGCGCGCCAC TGCCCTCCAG CCTGGGCAAC AGAGTGAGAC CCTGCCTCAA ACAAAAACGT 840 AAACAAAACA GGAGGCCCTG CTCTCCTGAG GGGCTGGTGG TGAGTCACTG GTAGATGGGA 900 GAGAGCTGGG GTCAGGGTCC CAGCTGGGGG GGTGGGTCCT CACCTGTGCT ACCCTCCAGG 960 GGGCCTCTCT CCAGGCCTCT GTCCCTCCCC TGGGAAGCCT GGCAGAAACC TGAGACTGGG 1020 CCTCCAGTTC CAGGTCGCCA CTGGGCCCAG GCCTCTCCTG TCCGCCTGCC AGGGACTGCG 1080 GAACAGGTAA CTCCTGCGCC ACCCTAAACC CACCTGGCCT GTTGCTCCAG GTGCGGCCTG 1140 GAGGCCCCGG GGCCTGCACA CCTGGTCAGC TCAGAGGCCA GGAAGAGGAG CGGAGGGAGG 1200 GGTGGGGCCG CCGGCCGCTG CTGGTTTCGT TTTGAGCCGG GCCCCTTCTT CCTCCCTCCC 1260 TCCCACTCCT CGCCAGACCC CTGCATTCTG GGAAAGGCTG TGACAACTTC CTCTGAACTC 1320 TCCTTAACCT GCCCTGGAGC CCAGGGCCTC CAGGAGGCTG AGTTCCGCCT GCGGGACCTG 1380 AGGCTTCCTG CAGGTCACAC ACCTCCACCC CTGGCCACGT GGCCCTAGAC CGCCCACCTT 1440 CTAGAAGCTT CTTTATGTGC TGCCCCATCA TGTCCCCACC CCGGGTGCAG CTGTCCCCTG 1500 CCTGCACCCC CTCCACCCTG TGTCCCAGAC TCTGCACACA GGAAACCGCC CTGGCCCCAG 1560 GGAGGGCTGC CTGAGACCCC CGCCTCCAAC CTGCACTGGG GACATCTGGG CTGGATGGTC 1620 CTCGGGAGGT GGGGCTGCCT TGGGCACTGC AGGGTGCTGG GTGACATCTC TGGCCTCCAT 1680 CCATTCCATG GCAGGGGCAC CCCCTGTCTC GACAACCACA GACGTCTGGG AGTTTCCAAG 1740 CCTCCCCTGG GTGGGGGGAC AGAATTGTTC CTGCTAAGAT CCAGTGGATT AAAAGACATC 1800 TGTGAGGGGA CAGAAATGAC 1820
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